Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.020 < 0.001 2 2012 2015
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2008 2008
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2008 2008
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs13281615
rs13281615 		0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs13281615
rs13281615 		0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs13281615
rs13281615 		0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs1562430
rs1562430 		0.807 0.160 8 127375606 intron variant T/C snv 0.41
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015
dbSNP: rs1562430
rs1562430 		0.807 0.160 8 127375606 intron variant T/C snv 0.41
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015
dbSNP: rs1562430
rs1562430 		0.807 0.160 8 127375606 intron variant T/C snv 0.41
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
Malignant neoplasm of gastrointestinal tract 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2017 2017
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
Differentiated Thyroid Gland Carcinoma 		0.010 < 0.001 1 2011 2011
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2018 2018
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
Primary differentiated carcinoma of thyroid gland 		0.010 < 0.001 1 2011 2011
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2018 2018
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.720 0.667 3 2008 2012
dbSNP: rs13254738
rs13254738 		0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.720 0.667 3 2008 2012
dbSNP: rs620861
rs620861 		0.925 0.080 8 127323428 intron variant G/A snv 0.36
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.030 0.667 3 2009 2017
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2011 2017
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2011 2017
dbSNP: rs620861
rs620861 		0.925 0.080 8 127323428 intron variant G/A snv 0.36
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.730 0.750 4 2008 2017
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.040 0.750 4 2008 2016
dbSNP: rs6983267
rs6983267 		0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.040 0.750 4 2008 2016
dbSNP: rs13281615
rs13281615 		0.716 0.360 8 127343372 intron variant A/G snv 0.43
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.800 0.850 20 2007 2016